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September 6th, 2008
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It's been a week and I haven't said anything to my coworkers about diabetes. Not even to either of my bosses. I'm not hiding it either. I really thought that on my first day people would be pointing and staring and asking about my pump, which I decided to wear on my belt as usual.

 

But nothing. I was surprised, actually. On day two or three, I was introduced to two people who I will work closely with in the future, one of whom noticed that something was on my belt, but she couldn't really figure out what it was. A cell phone? An iPod? she wondered aloud.

 

"It's an insulin pump," I said matter of factly.

 

"A what?"

 

"An insulin pump," I said.

 

"Oh."

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I debated where to wear Toohey today: in my pocket (out of sight) or on my belt as I always do. Prior to this morning, I had been to my new office three times: twice for interviews and once to sign my offer letter.* All three times Toohey was tucked neatly in my pocket, no tubing was visible, I was a normal-looking person.

 

So I debated for several days and ultimately decided not to hide, to wear Toohey on my belt as always, to be myself. I decided though to not come out and say "Hey, I have diabetes" on my first day. I just wanted it to flow, to just happen naturally. I really thought I would have had some questions since Toohey was so visible.

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Recently, a woman at work discovered I have diabetes. I don't hide the fact that I have it at work, but it's not readily apparent. In the interest of safety, I've told several key people outright - and the folks in the near vicinity of my work space know because I don't hide my testing, pumping, or other efforts toward good control. If someone asks, I am usually happy to answer questions, clear up misconceptions, or alleviate concerns.

L, who works on the other side of our fairly large office, and who I don't see that often, came to my desk the other day and rather unceremoniously started into a monologue about my diabetes, It went something like, "Oh, Nicole" Look of concern, "A just told me about your diabetes. You have the bad kind, don't you? You have to take shots and things. Oh it must be so hard with having it the way you do. You have to stay away from sweets and I bet the shots hurt a lot."

Oh Dear. What to do? (READ MORE)



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Kerri Morrone
Kerri Morrone, diagnosed with type 1 diabetes when she was six years old, doesn't let diabetes define her. It just helps explain some things.
Creator of the diabetes blog Six Until Me and an editor for dLife, Kerri is an awareness advocate and an active member of the diabetes community. She'd also like a kitten. (Read More)


Latest Posts: There Are No Rules! | Evidence | Pain Thresholds

Rebecca Abma
What happens when a health writer develops a chronic illness? As Rebecca K. Abma can tell you, it turns into an obsession. Since being diagnosed with type 2 diabetes in December 2003, 90 percent of her non-work computer time is spent researching the disease and chatting with fellow diabetics. (Read More)

Latest Posts: A Constant Reminder? | I Deserved That | Pumped Up!

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